HRP20100240T1 - Polipeptidi za indukciju zaštitnog imunitetnog odgovora protiv staphylococcus aureus - Google Patents

Polipeptidi za indukciju zaštitnog imunitetnog odgovora protiv staphylococcus aureus Download PDF

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HRP20100240T1
HRP20100240T1 HR20100240T HRP20100240T HRP20100240T1 HR P20100240 T1 HRP20100240 T1 HR P20100240T1 HR 20100240 T HR20100240 T HR 20100240T HR P20100240 T HRP20100240 T HR P20100240T HR P20100240 T1 HRP20100240 T1 HR P20100240T1
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seq
polypeptide
sequence
amino acid
immunogen
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S. Anderson Annaliesa
Ute Jansen Kathrin
Kelly Rosemarie
D. Schultz Loren
L. Montgomery Donna
L. Mcclements William
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Merck Sharp & Dohme Corp.
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/02Bacterial antigens
    • A61K39/085Staphylococcus
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2/00Peptides of undefined number of amino acids; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • AHUMAN NECESSITIES
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
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    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/04Immunostimulants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/195Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
    • C07K14/305Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Micrococcaceae (F)
    • C07K14/31Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Micrococcaceae (F) from Staphylococcus (G)
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K2319/00Fusion polypeptide
    • C07K2319/35Fusion polypeptide containing a fusion for enhanced stability/folding during expression, e.g. fusions with chaperones or thioredoxin

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Abstract

Polipeptidni imunogen, naznačen time što sadrži aminokiselinsku sekvencu koja je najmanje 90% identična sekvenci SEQ ID NO: 1, pri čemu navedeni polipeptid osigurava zaštitni imunitet protiv S. aureus i pri čemu, ako je prisutno jedna ili više dodatnih polipeptidnih regija, tada navedene dodatne regije ne osiguravaju karboksil terminus koji sadrži aminokiseline 609-645 sekvence SEQ ID NO: 2. Patent sadrži još 30 patentnih zahtjeva.

Claims (31)

1. Polipeptidni imunogen, naznačen time što sadrži aminokiselinsku sekvencu koja je najmanje 90% identična sekvenci SEQ ID NO: 1, pri čemu navedeni polipeptid osigurava zaštitni imunitet protiv S. aureus i pri čemu, ako je prisutno jedna ili više dodatnih polipeptidnih regija, tada navedene dodatne regije ne osiguravaju karboksil terminus koji sadrži aminokiseline 609-645 sekvence SEQ ID NO: 2.
2. Polipeptid prema patentnom zahtjevu 1, naznačen time što se navedeni polipeptid sastoji od aminokiselinske sekvence koja je najmanje 90% identična sekvenci SEQ ID NO: 3 ili njenog fragmenta koji sadrži aminokielinsku sekvencu koja je najmanje 90% identična sekvenci SEQ ID NO: 1.
3. Polipeptid prema patentnom zahtjevu 2, naznačen time što se navedeni polipeptid sastoji od aminokiselinske sekvence koja je najmanje 94% identična sekvenci SEQ ID NO: 3, ili njenog fragmenta koji sadrži aminokiselinsku sekvencu koja je najmanje 94% identična sekvenci SEQ ID NO: 1.
4. Polipeptid prema patentnom zahtjevu 3, naznačen time što se navedeni polipeptid sastoji od aminokiselinske sekvence koja je najmanje 94% identična sekvenci SEQ ID NO: 1, SEQ ID NO: 3 ili SEQ ID NO: 42.
5. Polipeptid prema patentnom zahtjevu 1, naznačen time što je navedeni polipeptid - SEQ ID NO: 1, SEQ ID NO: 3 ili SEQ ID NO: 42; ili se razlikuje od navedenih sekvenci prema maksimalno 25 aminokiselinskih zamjena.
6. Polipeptid prema patentnom zahtjevu 5, naznačen time što je navedeni polipeptid SEQ ID NO: 1, SEQ ID NO: 3 ili SEQ ID NO: 42, ili se razlikuje od navedenih sekvenci prema maksimalno 10 aminokiselinskih zamjena.
7. Polipeptid prema patentnom zahtjevu 6, naznačen time što je navedeni polipeptid SEQ ID NO: 1, SEQ ID NO: 3 ili SEQ ID NO: 42, ili se razlikuje od navedenih sekvenci prema maksimalno 5 aminokiselinskih zamjena.
8. Polipeptid prema patentnom zahtjevu 1 naznačen time što je navedeni polipeptid SEQ ID NO: 1, SEQ ID NO: 3 ili SEQ ID NO: 42.
9. Polipeptid prema patentnom zahtjevu 1 naznačen time što se navedeni polipeptid sastoji od aminokiselinske sekvence od SEQ ID NO 1, 3, 7, 17, 20 ili 42 i do 20 dodatnih aminokiselina.
10. Polipeptid prema patentnom zahtjevu 5, naznačen time što se navedeni polipeptid sastoji od aminokiselinske sekvence SEQ ID NO 7, 17 ili 20.
11. Polipeptid prema bilo kojem prethodnom patentnom zahtjevu, naznačen time što mu nedostaju svi, ili većina, drugih polipeptida sa kojim je ovaj polipeptid prirodno povezan.
12. Imunogen, naznačen time što se sastoji od polipeptida prema bilo kojem prethodnom patentnom zahtjevu, pri čemu se navedeni imunogen sastoji od navedene aminokiselinske sekvence i jedne ili više dodatnih regija ili grupa kovalentno vezanih za navedenu sekvencu na karboksil terminusu ili amino terminusu, pri čemu je svaka regija ili grupa nezavisno izabrana od regija ili grupe koji imaju najmanje jedno od slijedećih svojstava: pojačavaju imunitetni odgovor, olakšavaju pročišćavanje ili omogućavaju stabilnost polipeptida.
13. Kompozicija koja je sposobna da inducira zaštitni imunitetni odgovor kod pacijenta, naznačena time što sadrži imunitetno efikasnu količinu imunogena prema bilo kojem od patentnih zahtjeva 1-12 i farmaceutski prihvatljiv nosač.
14. Kompozicija prema patentnom zahtjevu 13, naznačena time što navedena kompozicija dalje sadrži adjuvant.
15. Nukleinska kiselina, naznačena time što sadrži rekombinantni gen koji sadrži nukleotidnu sekvencu koja kodira polipeptidni imunogen prema bilo kojem od patentnih zahtjeva 1-10.
16. Nukleinska kiselina prema patentnom zahtjevu 15, naznačena time što rekombinantni gen ne kodira sekvencu staničnog signalnog peptida i ne kodira signalnu sekvencu za sortiranje staničnog zida.
17. Nukleinska kiselina prema patentnom zahtjevu 16, naznačena time što navedeni rekombinantni gen sadrži jedan ili više kodona optimiziranih za ekspresiju kvasca.
18. Nukleinska kiselina prema patentnom zahtjevu 17, naznačena time što je navedena nukleotidna sekvenca najmanje 50% kodon-optimizirana za ekspresiju u kvascu.
19. Nukleinska kiselina prema patentnom zahtjevu 16, naznačena time što je navedena nukleotidna sekvenca izabrana iz grupe koju čine: SEQ ID NO: 30, SEQ ID NO: 31, SEQ ID NO: 32, SEQ ID NO: 33, SEQ ID NO: 34, SEQ ID NO: 35, SEQ ID NO: 36, SEQ ID NO: 37, SEQ ID NO: 38, SEQ ID NO: 39, SEQ ID NO: 40, SEQ ID NO: 41, SEQ ID NO: 46, SEQ ID NO: 47, SEQ ID NO: 48, SEQ ID NO: 49, SEQ ID NO: 50, SEQ ID NO: 51, SEQ ID NO: 52 i SEQ ID NO: 53.
20. Nukleinska kiselina prema patentnom zahtjevu 15 ili 19, naznačena time što je navedena nukleinska kiselina - ekspresioni vektor.
21. Rekombinantna stanica, naznačena time što sadrži nukleinsku kiselinu prema bilo kojem od patentnih zahtjeva 15-20.
22. Postupak za pripremu S. aureus polipeptida koji osigurava zaštitni imunitet, naznačen time što sadrži slijedeće korake: (a) rast rekombinantne stanice prema patentnom zahtjevu 21 pod uvjetima u kojima je polipeptid prema bilo kojem od patentnih zahtjeva 1 do 11 eksprimiran; i (b) pročišćavanje navedenog peptida.
23. Postupak prema patentnom zahtjevu 22, naznačena time što je navedena rekombinantna stanica S. cerevisiae.
24. Imunogen prema bilo kojem od patentnih zahtjeva 1 do 12, naznačen time što je namijenjen za primjenu u postupku liječenja ljudskog tijela putem terapije.
25. Imunogen prema patentnom zahtjevu 24, naznačen time što je namijenjen za osiguravanje zaštitnog imuniteta protiv S. aureus.
26. Imunogen prema patentnom zahtjevu 25, naznačen time što je navedeni pacijent čovjek.
27. Imunogen prema patentnom zahtjevu 25, naznačen time što se navedeni pacijent tretira profilaktički protiv S. aureus infekcije.
28. Imunogen prema patentnom zahtjevu 24, naznačen time što je namijenjen za indukciju anamnestičkog odgovora.
29. Imunogen prema patentnom zahtjevu 28, naznačen time što navedeni anamnestički odgovor ima za rezultat najmanje 3-struko povećanje u geometrijskom titru u odnosu na prethodni titar u roku od 3 dana.
30. Primjena imunogena prema bilo kojem od patentnih zahtjeva 1 do 12, naznačena time što je namijenjena za proizvodnju lijeka za primjenu u postupku kao što je definirano u bilo kojem od patentnih zahtjeva 25 do 29.
31. Imunogen prema bilo kojem od patentnih zahtjeva 1 do 12, naznačen time što je u kombinaciji sa dodatnim imunogenima koji su izabrani iz grupe koju čine: jedan ili više dodatnih imunogena S. aureus; jedan ili više imunogena koji ciljano djeluju na jedan ili više drugih organizama Staphylococcus; i jedan ili više imunogena koji ciljano djeluju na druge infektivne organizme.
HR20100240T 2003-07-24 2010-04-26 Polipeptidi za indukciju zaštitnog imunitetnog odgovora protiv staphylococcus aureus HRP20100240T1 (hr)

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US48984003P 2003-07-24 2003-07-24
US52011503P 2003-11-14 2003-11-14
PCT/US2004/023523 WO2005009379A2 (en) 2003-07-24 2004-07-22 Polypeptides for inducing a protective immune response against staphylococcus aureus

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US (2) US20060177462A1 (hr)
EP (1) EP1651166B8 (hr)
JP (1) JP2007502101A (hr)
KR (1) KR20060065643A (hr)
AT (1) ATE457737T1 (hr)
AU (1) AU2004258979B2 (hr)
BR (1) BRPI0412799A (hr)
CA (1) CA2532370A1 (hr)
CY (1) CY1110028T1 (hr)
DE (1) DE602004025579D1 (hr)
DK (1) DK1651166T3 (hr)
ES (1) ES2342778T3 (hr)
HR (1) HRP20100240T1 (hr)
IL (1) IL173253A0 (hr)
IS (1) IS8213A (hr)
MX (1) MXPA06000854A (hr)
NO (1) NO20060898L (hr)
NZ (2) NZ570750A (hr)
PL (1) PL1651166T3 (hr)
PT (1) PT1651166E (hr)
RU (1) RU2337108C2 (hr)
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WO (1) WO2005009379A2 (hr)

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WO2005009379A3 (en) 2006-11-30
BRPI0412799A (pt) 2006-09-26
NZ570750A (en) 2009-12-24
RU2337108C2 (ru) 2008-10-27
MXPA06000854A (es) 2006-03-30
US20100247561A1 (en) 2010-09-30
SI1651166T1 (sl) 2010-06-30
AU2004258979A1 (en) 2005-02-03
PL1651166T3 (pl) 2010-08-31
NO20060898L (no) 2006-04-24
EP1651166B1 (en) 2010-02-17
ATE457737T1 (de) 2010-03-15
EP1651166B8 (en) 2010-05-19
WO2005009379A2 (en) 2005-02-03
EP1651166A2 (en) 2006-05-03
JP2007502101A (ja) 2007-02-08
CA2532370A1 (en) 2005-02-03
RU2006105498A (ru) 2006-09-10
IL173253A0 (en) 2006-06-11
KR20060065643A (ko) 2006-06-14
AU2004258979B2 (en) 2007-12-06
NZ544542A (en) 2009-01-31
ES2342778T3 (es) 2010-07-14
EP1651166A4 (en) 2008-03-05
DK1651166T3 (da) 2010-05-31
IS8213A (is) 2005-12-30
CY1110028T1 (el) 2015-01-14
PT1651166E (pt) 2010-04-23
US20060177462A1 (en) 2006-08-10
DE602004025579D1 (de) 2010-04-01

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